ENST00000354968.5:c.488-261G>T
|
ENSP00000347055.1:n.488-261G>T
|
|
ENST00000393450.5:c.488-261G>T
MANE Select
|
ENSP00000377096.1:n.488-261G>T
|
|
ENST00000536623.6:c.488-261G>T
|
ENSP00000442375.2:n.488-261G>T
|
|
ENST00000570671.1:c.199-261G>T
|
|
|
ENST00000571981.5:c.*274-261G>T
|
ENSP00000459035.1:n.*274-261G>T
|
|
ENST00000572316.5:c.488-261G>T
|
ENSP00000461570.1:n.488-261G>T
|
|
ENST00000573747.6:c.*90-261G>T
|
ENSP00000460734.1:n.*90-261G>T
|
|
ENST00000576874.5:c.488-261G>T
|
ENSP00000458907.1:n.488-261G>T
|
|
NM_001002841.1:c.488-261G>T
|
NP_001002841.1:n.488-261G>T
|
|
NM_002476.2:c.488-261G>T
MANE Select
|
NP_002467.1:n.488-261G>T
|
|
XM_005257391.3:c.488-261G>T
|
XP_005257448.1:n.488-261G>T
|
|
XM_011524838.1:c.488-261G>T
|
XP_011523140.1:n.488-261G>T
|
|
XM_011524839.1:c.278-261G>T
|
XP_011523141.1:n.278-261G>T
|
|
XM_005257391.5:c.488-261G>T
|
XP_005257448.1:n.488-261G>T
|
|
XM_011524839.2:c.581-261G>T
|
XP_011523141.2:n.581-261G>T
|
|
XM_017024683.1:c.581-261G>T
|
XP_016880172.1:n.581-261G>T
|
|
XM_024450766.1:c.581-261G>T
|
XP_024306534.1:n.581-261G>T
|
|
NM_001002841.2:c.488-261G>T
|
NP_001002841.1:n.488-261G>T
|
|